Travaux scientifiques

Prof. Dr. Tülay Güran

389 publications. La source de l’information est indiquée à côté de chaque publication.

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  1. Long-term clinical outcomes of primary adrenal insufficiency caused by homozygous CYP11A1 p.R451W variant

    European Journal of Endocrinology, 2026

    DOI 10.1093/ejendo/lvag110 PMID 42340003 Texte intégral en libre accèsSource : OpenAlex

  2. Utility of a 40-minute LH level after depot leuprolide for diagnosis and treatment monitoring in girls with CPP

    Journal of endocrinological investigation, 2026

    DOI 10.1007/s40618-026-02925-0 PMID 42189483 Texte intégral en libre accèsSource : Europe PMC

  3. BMI-SDS Changes During GnRHa Therapy in 150 Girls with Idiopathic Central Precocious Puberty: Follow-up Through Final Height

    Journal of clinical research in pediatric endocrinology, 2026

    DOI 10.4274/jcrpe.galenos.2026.2026-3-6 PMID 42028850 1 citation (Europe PMC) Texte intégral en libre accèsSource : Europe PMC

  4. Isolated Hypoglycemia in Children with Cystic Fibrosis: Role of Pancreatic Insufficiency and Glucagon Response

    Journal of clinical research in pediatric endocrinology, 2026

    DOI 10.4274/jcrpe.galenos.2025.2025-2-6 PMID 41090401 Texte intégral en libre accèsSource : Europe PMC

  5. Isolated Hyperchlorhidrosis Caused by Novel Biallelic CA12 Variants Mimicking Pseudohypoaldosteronism

    2026

    DOI 10.1159/hrp/adaag054 Source : ORCID

  6. Machine learning algorithms to accelerate etiological diagnosis of congenital disorders of adrenal steroidogenesis

    The Journal of Clinical Endocrinology & Metabolism, 2026

    DOI 10.1210/clinem/dgag237 PMID 42359583 2 citations (Europe PMC) Texte intégral en libre accèsSource : ORCID

  7. Determinants of pubertal progression and final height in premature pubarche

    Journal of Endocrinological Investigation, 2026

    DOI 10.1007/s40618-026-02957-6 PMID 42340620 Texte intégral en libre accèsSource : ORCID

  8. Response to Letter to the Editor from Ting and Chen: “Impact of Growth-Promoting Therapies on Puberty, Growth, and Final Height in Classical 21-Hydroxylase Deficiency”

    The Journal of Clinical Endocrinology & Metabolism, 2026

    DOI 10.1210/clinem/dgag029 PMID 41711662 Source : ORCID

  9. Positive neonatal screening test for congenital adrenal hyperplasia in a case with 3β-hydroxysteroid dehydrogenase type 2 deficiency

    Journal of Pediatric Endocrinology and Metabolism, 2026

    DOI 10.1515/jpem-2025-0403 PMID 41111433 Source : ORCID

  10. The 40<sup>th</sup> Minute Cortisol Measurement is the Key Time-Point in the Low-Dose Synacthen Stimulation Test: A Large, Assay-Specific Pediatric Validation Study

    Journal of clinical research in pediatric endocrinology, 2026

    DOI 10.4274/jcrpe.galenos.2026.2026-1-17 PMID 42043277 Texte intégral en libre accèsSource : Europe PMC

  11. Adrenal androgens as predictors of growth characteristics in premature pubarche

    European journal of endocrinology, 2026

    DOI 10.1093/ejendo/lvag024 PMID 41637567 1 citation (Europe PMC) Source : Europe PMC

  12. Growth patterns and bone maturation in children with sex chromosomal (45,X/46,XY) differences of sex development

    European journal of endocrinology, 2026

    DOI 10.1093/ejendo/lvag092 PMID 42156235 Texte intégral en libre accèsSource : Europe PMC

  13. Contemporary global management of 21-hydroxylase deficiency congenital adrenal hyperplasia in early infancy: a multi-national registry study

    European journal of endocrinology, 2026

    DOI 10.1093/ejendo/lvag004 PMID 41531283 1 citation (Europe PMC) Texte intégral en libre accèsSource : Europe PMC

  14. How Accurate is Self-Reported Parental Height? Evidence From a Tertiary Pediatric Endocrinology

    Southern Clinics of Istanbul Eurasia, 2026

    DOI 10.14744/scie.2026.51333 Texte intégral en libre accèsSource : OpenAlex

  15. Growth Patterns and Bone Maturation in Children with Sex Chromosomal (45,X/46,XY) DSD.

    Open Access CRIS of the University of Bern, 2026

    DOI 10.48620/97945 Texte intégral en libre accèsSource : OpenAlex

  16. Premature Adrenarche Followed to Adolescence: PCOS Risk and Phenotype

    European Archives of Medical Research, 2026

    DOI 10.14744/eamr.2026.60566 Texte intégral en libre accèsSource : OpenAlex

  17. Broad spectrum of DSD with NR5A1 variants: challenges to address/confirm mechanisms of variable expressivity and incomplete penetrance

    Endocrine Abstracts, 2026

    DOI 10.1530/endoabs.118.po82 Source : OpenAlex

  18. Clinical Correlates of Adrenal Zona Reticularis Function in Turner Syndrome

    Figshare, 2026

    DOI 10.6084/m9.figshare.32780793 Texte intégral en libre accèsSource : OpenAlex

  19. Clinical Correlates of Adrenal Zona Reticularis Function in Turner Syndrome

    Figshare, 2026

    DOI 10.6084/m9.figshare.32780751 Texte intégral en libre accèsSource : OpenAlex

  20. Circulating mRNA and miRNA Signatures Used as Predictive Markers of Lifestyle Modification Outcomes in Pediatric Obesity Management

    Hormone Research in Paediatrics, 2026

    DOI 10.1159/000553090 PMID 42391183 Source : OpenAlex

  21. Diagnostic work-up in paediatric adrenocortical tumours: an international consensus

    European Journal of Endocrinology, 2026

    DOI 10.1093/ejendo/lvag086 PMID 42413072 Texte intégral en libre accèsSource : OpenAlex

  22. Differences of Sexual Development (DSD) and Gender Incongruence (GI)

    Yearbook of pediatric endocrinology, 2026

    DOI 10.1530/ey.23.6.0 Source : OpenAlex

  23. Comprehensive assessment of the genotype-phenotype spectrum and treatment for monoallelic insulin receptoropathy in a cohort of 505 people

    Research Square, 2026

    DOI 10.21203/rs.3.rs-10884175/v1 PMID 42856426 Texte intégral en libre accèsSource : OpenAlex

  24. Clinical and Genetic Heterogeneity of Triple A Syndrome: A Multicenter Study

    Hormone Research in Paediatrics, 2026

    DOI 10.1159/hrp/adaag030 PMID 42886620 Source : OpenAlex

  25. Comprehensive review of the genotype-phenotype spectrum and treatment for biallelic insulin receptoropathy based on 259 affected people

    Research Square, 2026

    DOI 10.21203/rs.3.rs-11296131/v1 Texte intégral en libre accèsSource : OpenAlex

  26. Oligogenic analysis across broad phenotypes of 46,XY differences in sex development associated with NR5A1/SF-1 variants: findings from the international SF1next study

    EBioMedicine, 2025

    DOI 10.1016/j.ebiom.2025.105624 PMID 40037090 9 citations (Europe PMC) Texte intégral en libre accèsSource : OpenAlex

  27. Impact of Growth-promoting Therapies on Puberty, Growth, and Final Height in Classical 21-hydroxylase Deficiency

    The Journal of Clinical Endocrinology & Metabolism, 2025

    DOI 10.1210/clinem/dgaf612 PMID 41349002 2 citations (Europe PMC) Source : OpenAlex

  28. Clinical and Molecular Spectrum of Infantile Hypercalcemia Type I: Insights Into CYP24A1 Variants

    Clinical Endocrinology, 2025

    DOI 10.1111/cen.70064 PMID 41327588 Source : OpenAlex

  29. The Mystery of Elevated β-hCG in GnRH-Independent Precocious Puberty without a Detectable Tumor: A Six-Year Diagnostic Odyssey

    Hormone Research in Paediatrics, 2025

    DOI 10.1159/000549889 PMID 41335548 Source : OpenAlex

  30. Real-life experience on efficacy and safety of setmelanotide treatment in prepubertal children

    European journal of endocrinology, 2025

    DOI 10.1093/ejendo/lvaf008 PMID 39891402 1 citation (Europe PMC) Source : Europe PMC

  31. Comparison of metabolic control in children with type 1 diabetes using reimbursed, self-funded intermittent, and self-funded continuous CGM

    Endocrine Abstracts, 2025

    DOI 10.1530/endoabs.110.p433 Source : OpenAlex

  32. Classification of bone turnover and calcium metabolism markers based on the molecular subtypes of osteogenesis imperfecta

    Endocrine Abstracts, 2025

    DOI 10.1530/endoabs.110.p207 Source : OpenAlex

  33. Response to the letter by Schmitt et al.

    European Journal of Endocrinology, 2025

    DOI 10.1093/ejendo/lvaf175 PMID 40838348 Source : ORCID

  34. Primary adrenal insufficiency caused by pseudo-neonatal adrenoleukodystrophy associated with biallelic ACOX1 mutations

    European Journal of Endocrinology, 2025

    DOI 10.1093/ejendo/lvaf094 PMID 40326779 1 citation (Europe PMC) Source : ORCID

  35. Primary adrenal insufficiency in patients with CPOX gene mutations

    European Journal of Endocrinology, 2025

    DOI 10.1093/ejendo/lvaf089 PMID 40296768 5 citations (Europe PMC) Source : ORCID

  36. Phenotypic Variation and Pubertal Outcomes in Males and Females with 46,XY Partial Gonadal Dysgenesis.

    The Endocrine Society, 2025

    DOI 10.17863/cam.117528 Texte intégral en libre accèsSource : ORCID

  37. Phenotypes linked to duplication upstream of SOX9: New insights into presentation and diagnosis

    The Journal of clinical endocrinology and metabolism, 2025

    DOI 10.1210/clinem/dgaf020 PMID 39812180 3 citations (Europe PMC) Texte intégral en libre accèsSource : ORCID

  38. Antenatal Diagnosis and Treatment in Congenital Adrenal Hyperplasia Due to 21-hydroxylase Deficiency and Congenital Adrenal Hyperplasia Screening in Newborns

    Journal of clinical research in pediatric endocrinology, 2025

    DOI 10.4274/jcrpe.galenos.2024.2024-6-10-s PMID 39713885 1 citation (Europe PMC) Texte intégral en libre accèsSource : Europe PMC

  39. Gonadal function and pathology in 17beta-HSD 3 and 5alpha-reductase deficiency

    European journal of endocrinology, 2025

    DOI 10.1093/ejendo/lvae154 PMID 39782875 4 citations (Europe PMC) Texte intégral en libre accèsSource : Europe PMC

  40. Expanding the Clinical Features of Schimke Immuno-osseous Dysplasia: a New Patient with a Novel Variant and Novel Clinical Findings

    Journal of clinical research in pediatric endocrinology, 2025

    DOI 10.4274/jcrpe.galenos.2024.2024-1-17 PMID 39113392 2 citations (Europe PMC) Texte intégral en libre accèsSource : Europe PMC

  41. The First-Year Outcomes of the Nationwide Neonatal CAH Screening in Türkiye: High Rate of False Positives for 21-Hydroxylase Deficiency and a Higher Detection Rate of Non-Classical Cases

    Journal of clinical research in pediatric endocrinology, 2025

    DOI 10.4274/jcrpe.galenos.2025.2024-9-11 PMID 40405612 2 citations (Europe PMC) Texte intégral en libre accèsSource : Europe PMC

  42. Phenotypic Variation and Pubertal Outcomes in Males and Females With 46,XY Partial Gonadal Dysgenesis

    The Journal of clinical endocrinology and metabolism, 2025

    DOI 10.1210/clinem/dgaf223 PMID 40208111 6 citations (Europe PMC) Texte intégral en libre accèsSource : Europe PMC

  43. Thyroid surgery in pediatric age: a 10-year experience at a single center and literature review

    Journal of Pediatric Endocrinology and Metabolism, 2025

    DOI 10.1515/jpem-2024-0464 PMID 39753228 2 citations (OpenAlex) Source : OpenAlex

  44. Optimal Low-Dose Synacthen Stimulation Test Sampling Time for Diagnosis of Adrenal Insufficiency Using Monoclonal Antibody Immunoassay

    Hormone Research in Paediatrics, 2025

    DOI 10.1159/000544945 PMID 40031891 2 citations (OpenAlex) Source : OpenAlex

  45. Children With Diabetes and At Least One Non-Autoimmune Feature Should Be Considered for Monogenic Diabetes Testing

    The Journal of Clinical Endocrinology & Metabolism, 2025

    DOI 10.1210/clinem/dgaf430 PMID 40746173 2 citations (OpenAlex) Texte intégral en libre accèsSource : OpenAlex

  46. Outcomes and fertility in men with PAIS worldwide: lessons from an I-DSD registry platform cohort

    Endocrine Abstracts, 2025

    DOI 10.1530/endoabs.110.p1025 Source : OpenAlex

  47. Diagnostic work-up of paediatric adrenocortical tumours - International consensus through a modified Delphi process

    Endocrine Abstracts, 2025

    DOI 10.1530/endoabs.110.p78 Source : OpenAlex

  48. Growth-promoting therapy in congenital adrenal hyperplasia due to 21-hydroxylase deficiency: Real-world data from the I-CAH registry

    Endocrine Abstracts, 2025

    DOI 10.1530/endoabs.110.p62 Source : OpenAlex

  49. Genotype-phenotype correlation of patients with androgen insensitivity syndrome: a cohort study including 9 families

    Endocrine Abstracts, 2025

    DOI 10.1530/endoabs.110.ep1319 Source : OpenAlex

  50. SAT-171 Outcomes and fertility in men with PAIS worldwide : Lessons from an I-DSD Registry platform cohort

    Journal of the Endocrine Society, 2025

    DOI 10.1210/jendso/bvaf149.2020 Texte intégral en libre accèsSource : OpenAlex